Henipavirus: Difference between revisions

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'''Henipavirus''' is a genus of [[RNA virus]]es in the family [[Paramyxoviridae]], order [[Mononegavirales]]. Henipaviruses are zoonotic pathogens, which means they are transmitted from animals to humans. The genus includes several species, notably the [[Hendra virus]] and the [[Nipah virus]], both of which are known for causing severe disease in animals and humans, including respiratory and neurological diseases that can be fatal.
= Henipavirus =


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[[File:CSIRO_ScienceImage_1718_The_Hendra_Virus.jpg|thumb|right|Hendra virus, a type of Henipavirus]]
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==Etiology==
'''Henipavirus''' is a genus of [[viruses]] in the family [[Paramyxoviridae]], order [[Mononegavirales]], containing five established species: [[Hendra virus]], [[Nipah virus]], [[Cedar virus]], [[Mojang virus]], and [[Ghanaian bat virus]]. These viruses are known for their zoonotic potential, meaning they can be transmitted from animals to humans, often with severe consequences.
Henipaviruses are enveloped, negative-sense, single-stranded RNA viruses. Their genomes are approximately 18,000 to 19,000 nucleotides long. The virus particles are pleomorphic, ranging from spherical to filamentous shapes. The genome encodes several structural and non-structural proteins, including the fusion (F) protein and the attachment (G) protein, which play critical roles in the virus's ability to infect host cells.


==Epidemiology==
== Virology ==
Henipaviruses were first identified in the 1990s, with Hendra virus emerging in Australia and Nipah virus in Malaysia. Since then, outbreaks have been reported in several countries, primarily in Southeast Asia and Australia. The natural reservoirs of Henipaviruses are fruit bats, specifically species belonging to the genus ''[[Pteropus]]'', also known as flying foxes. These bats can transmit the virus to other animals, such as pigs, horses, and humans, through direct contact or indirectly through contaminated food or environments.


==Clinical Features==
[[File:Henipavirus_structure.svg|thumb|left|Structure of a Henipavirus]]
In humans, Henipavirus infections can range from asymptomatic to severe, often fatal, disease. Symptoms typically begin with fever, headache, and dizziness, progressing to more severe respiratory or neurological symptoms. In severe cases, encephalitis, seizures, and coma can occur, leading to death. The case fatality rate for Nipah virus infection can be as high as 75% in some outbreaks.
Henipaviruses are [[enveloped viruses]] with a non-segmented, negative-sense [[RNA genome]]. The genome is approximately 18,000 nucleotides in length and encodes six structural proteins. The viral envelope is derived from the host cell membrane and contains two major glycoproteins: the attachment glycoprotein (G) and the fusion glycoprotein (F), which are essential for viral entry into host cells.


==Diagnosis==
=== Genome ===
Diagnosis of Henipavirus infection is based on clinical symptoms, epidemiological factors, and laboratory tests. Laboratory diagnosis can be made through the detection of viral RNA by [[RT-PCR]], virus isolation, or serological methods to detect specific antibodies. However, these tests require biosafety level 4 (BSL-4) laboratories due to the high virulence and lack of treatment or vaccines for Henipavirus infections.


==Treatment and Prevention==
[[File:Henipavirus_genome.png|thumb|right|Genome organization of Henipavirus]]
There is currently no specific treatment or vaccine available for Henipavirus infections. Management of infected individuals primarily involves supportive care, including maintaining hydration and treating any secondary infections. Prevention strategies focus on reducing the risk of transmission from bats to humans and include avoiding contact with bats and their habitats, not consuming raw date palm sap, and implementing biosecurity measures in pig farms and other potential intermediate hosts.
The genome of Henipaviruses is organized into six genes, which encode the nucleocapsid protein (N), phosphoprotein (P), matrix protein (M), fusion protein (F), glycoprotein (G), and the large polymerase protein (L). The P gene also encodes additional proteins through RNA editing, including the V and W proteins, which are involved in evading the host immune response.


==Research and Future Directions==
== Transmission ==
Research on Henipaviruses is focused on understanding the virus's transmission dynamics, pathogenesis, and immune responses in hosts. Efforts are also underway to develop effective vaccines and antiviral therapies. The emergence of Henipaviruses as significant public health threats underscores the importance of surveillance, research, and preparedness to address zoonotic diseases.
Henipaviruses are primarily transmitted to humans through contact with infected animals or their secretions. [[Fruit bats]] of the family [[Pteropodidae]] are natural reservoirs for these viruses. Human infections have been associated with exposure to infected horses (Hendra virus) or pigs (Nipah virus), as well as direct contact with bat secretions.


[[Category:Virology]]
== Clinical Features ==
In humans, Henipavirus infections can cause severe respiratory illness and [[encephalitis]]. The incubation period varies, but symptoms typically begin with fever, headache, and myalgia, progressing to more severe neurological symptoms in some cases. The case fatality rate is high, particularly for Nipah virus infections.
 
== Prevention and Control ==
Preventive measures focus on reducing the risk of transmission from animals to humans. This includes avoiding contact with sick animals, implementing biosecurity measures in animal husbandry, and educating at-risk populations. There is currently no specific antiviral treatment for Henipavirus infections, but supportive care and intensive medical management are critical.
 
== Research and Development ==
[[File:Journal.pone.0199534.g001.A.png|thumb|left|Research on Henipavirus]]
Research is ongoing to develop vaccines and therapeutics for Henipavirus infections. The development of a vaccine for Hendra virus has been successful in horses, which helps prevent transmission to humans. Efforts are also underway to develop vaccines for Nipah virus and other Henipaviruses.
 
== Related Pages ==
* [[Paramyxoviridae]]
* [[Zoonosis]]
* [[Viral encephalitis]]
* [[RNA virus]]
 
[[Category:Paramyxoviridae]]
[[Category:Zoonoses]]
[[Category:Zoonoses]]
[[Category:Infectious diseases]]
[[Category:RNA viruses]]
{{medicine-stub}}
<gallery>
File:CSIRO ScienceImage 1718 The Hendra Virus.jpg|The Hendra Virus
File:CSIRO ScienceImage 1719 Hendra Virus.jpg|Hendra Virus
File:''Paramyxoviridae''.|Paramyxoviridae
File:Henipavirus structure.svg|Henipavirus Structure
File:Henipavirus genome.png|Henipavirus Genome
File:Journal.pone.0199534.g001.A.png|Henipavirus
</gallery>

Latest revision as of 14:15, 21 February 2025

Henipavirus[edit]

Hendra virus, a type of Henipavirus

Henipavirus is a genus of viruses in the family Paramyxoviridae, order Mononegavirales, containing five established species: Hendra virus, Nipah virus, Cedar virus, Mojang virus, and Ghanaian bat virus. These viruses are known for their zoonotic potential, meaning they can be transmitted from animals to humans, often with severe consequences.

Virology[edit]

Structure of a Henipavirus

Henipaviruses are enveloped viruses with a non-segmented, negative-sense RNA genome. The genome is approximately 18,000 nucleotides in length and encodes six structural proteins. The viral envelope is derived from the host cell membrane and contains two major glycoproteins: the attachment glycoprotein (G) and the fusion glycoprotein (F), which are essential for viral entry into host cells.

Genome[edit]

Genome organization of Henipavirus

The genome of Henipaviruses is organized into six genes, which encode the nucleocapsid protein (N), phosphoprotein (P), matrix protein (M), fusion protein (F), glycoprotein (G), and the large polymerase protein (L). The P gene also encodes additional proteins through RNA editing, including the V and W proteins, which are involved in evading the host immune response.

Transmission[edit]

Henipaviruses are primarily transmitted to humans through contact with infected animals or their secretions. Fruit bats of the family Pteropodidae are natural reservoirs for these viruses. Human infections have been associated with exposure to infected horses (Hendra virus) or pigs (Nipah virus), as well as direct contact with bat secretions.

Clinical Features[edit]

In humans, Henipavirus infections can cause severe respiratory illness and encephalitis. The incubation period varies, but symptoms typically begin with fever, headache, and myalgia, progressing to more severe neurological symptoms in some cases. The case fatality rate is high, particularly for Nipah virus infections.

Prevention and Control[edit]

Preventive measures focus on reducing the risk of transmission from animals to humans. This includes avoiding contact with sick animals, implementing biosecurity measures in animal husbandry, and educating at-risk populations. There is currently no specific antiviral treatment for Henipavirus infections, but supportive care and intensive medical management are critical.

Research and Development[edit]

Research on Henipavirus

Research is ongoing to develop vaccines and therapeutics for Henipavirus infections. The development of a vaccine for Hendra virus has been successful in horses, which helps prevent transmission to humans. Efforts are also underway to develop vaccines for Nipah virus and other Henipaviruses.

Related Pages[edit]